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Comparison of adherence of skin graft to wound and its survival with and without adjuvant negative pressure dressing.

Comparison of skin graft take with and without post grafting topical negative pressure dressing in patients requiring skin graft coverage to wound on lower limb.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001181493
Enrollment
80
Registered
2025-10-29
Start date
2025-03-01
Completion date
2025-08-20
Last updated
2025-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

To measure mean of skin graft take with and without post graft negative pressure wound dressing, in patients needing skin graft coverage for wounds involving lower limbs. Hypothetically The mean of skin graft take is higher with the use of post-grafting negative pressure wound therapy (NPWT) in patients needing skin graft for wound coverage in lower limbs compared to conventional dressings. NPWT continuously drains excess fluid, preventing seroma and hematoma formation. It Ensures better graft adherence by reducing shear forces, reduces bacterial load and inflammation, promoting a conducive healing environment, promotes micro vascularization crucial in compromised wounds, Improves graft success, minimizing the need for additional grafts and reducing donor site complications. This study aims to compare skin graft take in patients treated with and without NPWT post-grafting, providing evidence for NPWT’s potential benefits.

Interventions

All cases will be done under general anesthesia or spinal anesthesia by plastic surgeon in hospital operation theatre. In intervention group wound bed will be prepared by wound wash and debridement, skin graft will be harvested from the thigh and spread on derma carrier (1:1.5) then meshed with skin graft mesher. Skin graft will be deployed on wound and secured in place with surgical staples. Non adhesive perforated layer (paraffin gauze) will be applied on skin graft, then fluffed sterile gauz

All cases will be done under general anesthesia or spinal anesthesia by plastic surgeon in hospital operation theatre. In intervention group wound bed will be prepared by wound wash and debridement, skin graft will be harvested from the thigh and spread on derma carrier (1:1.5) then meshed with skin graft mesher. Skin graft will be deployed on wound and secured in place with surgical staples. Non adhesive perforated layer (paraffin gauze) will be applied on skin graft, then fluffed sterile gauze will be applied over paraffin gauze and suction device will be attached which will maintain constant negative pressure of -125mmHg. Change of dressing will be done on 5th post-operative day. Details of the skin grafting procedure will be recorded, including graft type, size, and location.

Sponsors

Combined military hospital Rawalpindi
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Healthy volunteers
No

Inclusion criteria

Patients of all age groups with wounds suitable for skin grafting involving lower limb, including traumatic wounds, post burn defects, chronic ulcers, post infection soft tissue defects

Exclusion criteria

Patients with psychiatric illnesses that may interfere with study participation. Immunocompromised patients (e.g., HIV/AIDS, on immunosuppressive therapy). Patients with active malignancies. Patients with ischemic wounds not suitable for grafting. Patients with deranged coagulation profiles (e.g., INR > 1.5, platelet count < 50,000/µL).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026